Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Apol7e |
G |
A |
15: 77,602,236 (GRCm39) |
R278H |
probably benign |
Het |
Arhgef17 |
A |
G |
7: 100,578,111 (GRCm39) |
S946P |
probably benign |
Het |
Capsl |
A |
T |
15: 9,462,689 (GRCm39) |
R110* |
probably null |
Het |
Ddx41 |
G |
A |
13: 55,682,293 (GRCm39) |
R205W |
possibly damaging |
Het |
Dock8 |
T |
A |
19: 25,160,368 (GRCm39) |
I1757N |
possibly damaging |
Het |
Dthd1 |
T |
C |
5: 62,996,580 (GRCm39) |
|
probably benign |
Het |
Eif5a2 |
A |
G |
3: 28,836,325 (GRCm39) |
E42G |
possibly damaging |
Het |
Elovl3 |
A |
G |
19: 46,121,639 (GRCm39) |
S61G |
probably benign |
Het |
Elp4 |
T |
C |
2: 105,672,677 (GRCm39) |
N136S |
probably benign |
Het |
Elp6 |
A |
G |
9: 110,149,886 (GRCm39) |
S223G |
probably benign |
Het |
Eml1 |
T |
A |
12: 108,503,675 (GRCm39) |
D743E |
probably damaging |
Het |
Ezh2 |
T |
C |
6: 47,535,194 (GRCm39) |
Q85R |
probably damaging |
Het |
Fermt3 |
C |
A |
19: 6,991,530 (GRCm39) |
C194F |
probably damaging |
Het |
Flg |
A |
G |
3: 93,200,260 (GRCm39) |
|
probably benign |
Het |
Gfi1b |
C |
T |
2: 28,500,186 (GRCm39) |
G282R |
probably damaging |
Het |
Gpr176 |
A |
T |
2: 118,109,927 (GRCm39) |
I444K |
probably benign |
Het |
Gys2 |
A |
T |
6: 142,408,970 (GRCm39) |
M95K |
possibly damaging |
Het |
Hgs |
C |
T |
11: 120,370,474 (GRCm39) |
R167W |
probably damaging |
Het |
Map3k20 |
T |
C |
2: 72,198,784 (GRCm39) |
I130T |
probably damaging |
Het |
Nckap5 |
A |
T |
1: 126,456,489 (GRCm39) |
Y25N |
probably damaging |
Het |
Npc1 |
C |
T |
18: 12,335,240 (GRCm39) |
V629I |
probably benign |
Het |
Nrl |
C |
A |
14: 55,759,909 (GRCm39) |
S6I |
probably damaging |
Het |
Or10am5 |
A |
T |
7: 6,517,741 (GRCm39) |
M229K |
probably benign |
Het |
Or4c29 |
T |
A |
2: 88,739,813 (GRCm39) |
D308V |
probably benign |
Het |
Or5d37 |
T |
C |
2: 87,924,178 (GRCm39) |
N34S |
probably benign |
Het |
Oxct2b |
T |
C |
4: 123,011,211 (GRCm39) |
F377S |
probably damaging |
Het |
Plb1 |
T |
C |
5: 32,427,162 (GRCm39) |
S91P |
probably benign |
Het |
Plxna2 |
C |
T |
1: 194,431,625 (GRCm39) |
S538F |
probably damaging |
Het |
Postn |
A |
T |
3: 54,292,644 (GRCm39) |
Y737F |
probably damaging |
Het |
Serpina1e |
T |
A |
12: 103,917,388 (GRCm39) |
I94F |
possibly damaging |
Het |
Serpine2 |
A |
G |
1: 79,788,265 (GRCm39) |
|
probably benign |
Het |
Stox2 |
T |
C |
8: 47,645,013 (GRCm39) |
R816G |
probably damaging |
Het |
Tep1 |
T |
C |
14: 51,071,024 (GRCm39) |
N2092D |
possibly damaging |
Het |
Tmem186 |
A |
G |
16: 8,453,748 (GRCm39) |
V171A |
probably benign |
Het |
Trim58 |
G |
A |
11: 58,533,934 (GRCm39) |
V163M |
probably benign |
Het |
Trim59 |
G |
T |
3: 68,945,162 (GRCm39) |
C59* |
probably null |
Het |
Ulk1 |
C |
T |
5: 110,937,223 (GRCm39) |
R691Q |
probably benign |
Het |
Vill |
A |
G |
9: 118,894,965 (GRCm39) |
N61S |
probably benign |
Het |
Zer1 |
C |
T |
2: 29,991,834 (GRCm39) |
R662H |
probably damaging |
Het |
Zfp644 |
A |
C |
5: 106,782,822 (GRCm39) |
V1184G |
probably benign |
Het |
Zfp974 |
A |
G |
7: 27,609,866 (GRCm39) |
S620P |
possibly damaging |
Het |
|
Other mutations in Gvin-ps3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00971:Gvin-ps3
|
APN |
7 |
105,681,008 (GRCm39) |
exon |
noncoding transcript |
|
IGL01125:Gvin-ps3
|
APN |
7 |
105,682,021 (GRCm39) |
missense |
unknown |
0.00 |
IGL01392:Gvin-ps3
|
APN |
7 |
105,682,962 (GRCm39) |
missense |
probably benign |
0.01 |
R1184:Gvin-ps3
|
UTSW |
7 |
105,683,159 (GRCm39) |
missense |
probably benign |
0.03 |
R1411:Gvin-ps3
|
UTSW |
7 |
105,682,686 (GRCm39) |
missense |
probably benign |
0.39 |
R2198:Gvin-ps3
|
UTSW |
7 |
105,682,758 (GRCm39) |
missense |
probably benign |
0.00 |
R2380:Gvin-ps3
|
UTSW |
7 |
105,681,374 (GRCm39) |
missense |
possibly damaging |
0.86 |
R3825:Gvin-ps3
|
UTSW |
7 |
105,682,780 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4397:Gvin-ps3
|
UTSW |
7 |
105,682,130 (GRCm39) |
exon |
noncoding transcript |
|
R4693:Gvin-ps3
|
UTSW |
7 |
105,681,585 (GRCm39) |
exon |
noncoding transcript |
|
R4787:Gvin-ps3
|
UTSW |
7 |
105,681,041 (GRCm39) |
exon |
noncoding transcript |
|
R4840:Gvin-ps3
|
UTSW |
7 |
105,680,627 (GRCm39) |
exon |
noncoding transcript |
|
R4972:Gvin-ps3
|
UTSW |
7 |
105,682,521 (GRCm39) |
exon |
noncoding transcript |
|
R5221:Gvin-ps3
|
UTSW |
7 |
105,683,181 (GRCm39) |
exon |
noncoding transcript |
|
R5296:Gvin-ps3
|
UTSW |
7 |
105,681,055 (GRCm39) |
exon |
noncoding transcript |
|
|